Prader-Willi Syndrome: Clinical Aspects

Prader-Willi Syndrome: Clinical Aspects

Prader-Willi Syndrome (PWS) is a complex multisystem genetic disorder that shows great variability, with changing clinical features during a patient's life. The syndrome is due to the loss of expression of several genes encoded on the proximal long arm of chromosome 15 (15q11.2–q13). The comple...

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Bibliographic Details
Main Authors: Elena, Grechi, Bruna, Cammarata, Benedetta, Mariani, Stefania, Di Candia, Giuseppe, Chiumello
Format: Online
Language:English
Published: Hindawi Publishing Corporation 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3486015/

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3486015/

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